Storage and handling
Other information Protect this product from excessive heat and sun. Do not use if seal is broken.
BENOVA PAIN AND ITCH RELIEF
- Manufacturer
- BENOVA RX LLC
- Effective date
- 2025-10-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:22:57
Label at a glance#
ProductBENOVA PAIN AND ITCH RELIEF
Active ingredientMENTHOL
Label structure10 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient Purpose
Menthol, 0.11%...........Topical analgesic, antipruritic
OTC - PURPOSE SECTION
Uses
For temporary relief of pain & itching associated with insect bites, sunburn, minor cuts, scrapes, minor skin irritations, and fever blisters & cold sores.
OTC - WHEN USING SECTION
Warnings
For external use only.
Avoid contact with eyes.
Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product & consult a doctor.
DOSAGE & ADMINISTRATION SECTION
Directions
Adults and children 2 years of age and older: Apply to affected area not more than 3 or 4 times daily. Children under 2 years of age: Do not use, consult
a doctor.
STORAGE AND HANDLING SECTION
Other information
Protect this product from excessive heat and sun.
Do not use if seal is broken.
INACTIVE INGREDIENT SECTION
Inactive ingredients
Water, Cyclopentasiloxane, Dimethicone, Dimethi- cone/PEG-10/15 Crosspolymer, Potassium Sorbate, Dimethicone/Vinyl Dimethicone Crosspolymer, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Actinidia Deliciosa, Brazilian Peppertree Extract (Schinus terebinthifolius), Red Root Extract (Ceanothus americanus), Licorice Root Extract, Bromelain, Nisin, Sodium Bicarbonate, Disodium EDTA, Sodium Hydroxide, Citric Acid.
WARNINGS SECTION
Warnings
For external use only.
Avoid contact with eyes.
Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product & consult a doctor.
Keep out of reach of children. If swallowed,get medical help or contact a Poison Control Center right away.
INDICATIONS & USAGE SECTION
Directions
Adults and children 2 years of age and older: Apply to affected area not more than 3 or 4 times daily. Children under 2 years of age: Do not use, consult a doctor.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Benova®
Pain & Itch
Relief Lotion
+Immediate Relief
+Steroid-Free Relief
+Gentle On Sensitive Skin
3 FL OZ (90 mL)
See uploaded image Benova_PainItchReliefLotion_3floz_PeelBack_FullLabel.jpg.
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0860008040763 | GTIN-13: 0860008040763 EAN-13: 0860008040763 GTIN-12: 860008040763 UPC-A: 860008040763 GTIN storage (14 digits): 00860008040763 | Benova_PainItchReliefLotion_3floz_PeelBack_FullLabel.jpg |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87150-001-03 | BENOVA PAIN AND ITCH RELIEF | 90 mL in 1 BOTTLE, WITH APPLICATOR | LOTION | 90 | 1 |
Products#
Every source-derived product name is available through these pages.
- BENOVA PAIN AND ITCH RELIEF
- MENTHOL, 0.11%
- POTASSIUM SORBATE
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)
- BRAZILIAN PEPPER
- SODIUM BICARBONATE
- EDETATE DISODIUM
- DIMETHICONE/PEG-10/15 CROSSPOLYMER
- WATER
- SODIUM HYDROXIDE
- MENTHOL
- ACTINIDIA DELICIOSA (KIWI) FRUIT
- CEANOTHUS AMERICANUS LEAF
- DIMETHICONE
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE
- CITRIC ACID
- LICORICE
- BROMELAIN
- NISIN
- CYCLOPENTASILOXANE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 87150-001 | 87150-001-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| BENOVA PAIN AND ITCH RELIEF | MENTHOL, 0.11% | BENOVA RX LLC | 42513ee2-8b40-a9f3-e063-6394a90a9386 | 2025-10-29 | Warnings | 87150-001-03 87150-001 87150000103 42513ee2-8b41-a9f3-e063-6394a90a9386 42513ee2-8b40-a9f3-e063-6394a90a9386 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.